O Raoul

[Spectral karyotyping (SKY) principle, avantages and limitations].

D Sanlaville, M Vekemans, S P Romana, 2003, Annales de biologie clinique.

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

R Redon, D Sanlaville, L Colleaux, 2006, Journal of Medical Genetics.

Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis.

J L Blouin, O Raoul, S. Antonarakis, 1994, American journal of human genetics.

19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation

C Turleau, L Colleaux, M Vekemans, 2009, Journal of Medical Genetics.